http://www.newscientistjobs.com/jobsNew Scientist Jobshttp://www.newscientistjobs.com/jobs/job/sas-programmer-for-a-large-cro-germany-200640315.htmTue, 17 Nov 2009 10:34:22 +0000187235SAS Programmer for a large CRO! An exciting opportunity has arisen with our client, a large CRO in their Germany site to join their quickly expanding Biostatistics and Programming department and take on a role of SAS Programmer! This challenging opportunity would be an ideal match for a professional within the industry who is fluent is fluent in both English and German. As a SAS Programmer you will be reporting to the VP of global biostatistics and programming and will be highly responsible for biostatistical activities of clinical trial projects assigned under consideration of the regulatory requirements, ICH and other international guidelines. An essential part of this role will be generating, evaluating and validating SAS programmed as required within the evaluation process. This will also include plausibility checks and other quality control actions in biostatistical areas. The ideal candidate will have a degree in medical sciences documentation or equivalent education. You will have a good knowledge of natural sciences and medical terminology and last but not least advanced knowledge of SAS software, including SAS Macro Language. This role will ideally fit to a professional with a good knowledge of coding of adverse events and a good experience in regulations and international guidelines. For more information about this excellent opportunity do not hesitate to contact Marketa Smelhausova on 0044 (0) 207 940 2103 or alternatively send an email on m.smelhausova@nonstop-pharma.com. http://www.newscientistjobs.com/jobs/job/director-or-drug-safety-germany-200631875.htmThu, 05 Nov 2009 15:54:04 +0000169067A Pharma company which has been established within the market for the past 15 years, is seeking a Director of Drug Safety to join their growing international organisation. This is a fantastic opportunity to be involved in a hierarchy in which you will be reporting straight into the Vice President. Also, joining at this time will enable you to be part of an excelling pipeline. The client is seeking a Medical Doctor with extensive experience in pharmacovigilance. People management responsibilities are not essential. You must be a team player, conscientious and highly self-motivated individual who enjoys establishing and maintaining good working relationships. For further information please forward your CV details to manpreet.mangat@SECpharma.com or alternatively call Manpreet Mangat on 0044 (0) 207 255 6600 SEC Recruitment Limited is acting as an Employment Agency and/or Employment Business http://www.newscientistjobs.com/jobs/job/pricing-reimbursement-manager-germany-200629085.htmTue, 03 Nov 2009 14:27:21 +0000171398My client is a respected international pharmaceutical company headquartered in Germany. We are currently assisting them in recruiting a Pricing & Reimbursement Manager for their headquarters. Job Description * Providing advice on the commercialisation of their products with a specific focus on pricing & reimbursement systems and how they impact on marketing and market access strategy * Assessing risk within pricing and market access with respect to price changes. You will have a particular focus on cross-border impacts. * Developing global pricing strategy and then communicating this to international teams. * Modelling of pricing scenarios and pricing impacts * Supporting the management team in the ongoing implementation of the company pricing and reimbursement process * You will develop pricing studies to assess the value held in existing products * You will assess and advocate the value proposition to international payers * Work with Business Development to target suitable opportunities * Act as a contact person for pricing & reimbursement questions for both internal and external stakeholders Skills * University degree in medicine/science/economics, preferably with a business or economics qualification * At least 2 years experience in role working in the pricing and reimbursement area either with a pharmaceutical firm or in a pricing and reimbursement consulting firm * Demonstrated expertise with pricing and reimbursement of pharmaceuticals with in depth knowledge of European pricing and reimbursement systems * Health care industry experience and in-depth knowledge of the pharmaceutical business including R&D, clinical and marketing * Strong ability to assess the economical and healthcare political environment and a keen sense to anticipate new trends and market opportunities * An excellent written and oral command of English * High degree of computer literacy and knowledge of computer modelling * Excellent analytical skills, judgment and problem solving skills Stelfox is a specialist provider of recruitment services within the Health Economics, Pricing & Market Access markets. http://www.newscientistjobs.com/jobs/job/senior-drug-safety-take-part-in-thier-growing-global-success-germany-200627190.htmMon, 02 Nov 2009 16:00:18 +0000163729A constantly growing International CRO with an increasing pipeline of new projects and internal promotions they are now seeking a Senior Drug Safety professional to be part of thier success. You will will be involved in managing individual case reports (SAEs, ADRs), reconciliation of SAEs, coding and data retrievals from the safety database, supporting the generation of periodic safety reports, and DSMB/DMC reviews. You will be involved in the safety management team and interfacing with the client and project team. You will also participate in responsibilities which range from signal generation activities to being responsible for ensuring relevant case reconciliation; Provision of line listings and tabulations for safety reports i.e. periodic safety reports, ad hoc safety reports etc. Qualifications An educational background in life sciences will be essential with the addition of having worked in a similar role, with an understanding of regulations relevant to the safety of drugs in development and post authorizations, as well as knowledge of clinical research. Ideally you have experience in effectively coaching and mentoring less experienced safety associates. Fluency in English is required and German is a plus. If you would to discuss this role in greater detail or your application / suitability to this or further roles, please call me or email me in confidence. If you are not available or suited to this position, please feel free to pass my details on. SEC Pharma People are acting as an Agency and or Employment Business For a confidential consultation call Manpreet Mangat on 0044 (0) 207 255 6600 or email your CV to manpreet.mangat@SECpharma.com SEC Recruitment Limited is acting as an Employment Agency and/or Employment Business http://www.newscientistjobs.com/jobs/job/reagulatory-affairs-manager-be-a-leader-germany-germany-200626002.htmMon, 02 Nov 2009 12:10:14 +0000163333REGULATORY AFFAIRS MANAGER - GERMANY - WORLDWIDE REGULATORY - LEADERSHIP, Based in the heart of of beautiful surroundings and easily accessible by surrounding European countries, our client is an established global pharmaceutical company. Being a family run business, the ethos and ethical stance this company has can not be matched by any other. Strong brand image matched with a strong product pipeline make this a great company to work for. You will manage a team of several employees dealing with global regulatory activities outside the European Union and North America. This will be registrations and post marketing on a global scale. Your team will be pivotal issues in your area of responsibility of contact for the other departments of the company and the responsibilities included: * Development of regulatory strategies and provide regulatory support, such as collection of registration documentation, in close cooperation with the participating departments * Collecting, interpreting and updating the registration requirements in the areas of Africa, Asia & Pacific, Middle and Far East, Eastern Europe, Latin America * Implementation of licensing procedures, modification and renewal for our drug ads * Developing and maintaining links with international partners and regulatory agencies Qualifications: * a degree in pharmacy, biology or chemistry have graduated with above-average success, a Ph.D. is desirable * Strong knowledge and experience in global registrations as well as post marketing. * very good English language skills and good MS Office skills, have an additional foreign language is desirable For more information regarding this vacancy please contact the Senior Consultant Abid Kanji on 0207 940 2108 or email him at regulatory@nonstop-pharma.com